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FDA 510(k)

PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350)

K-Number: K890198 · 1989-06-12

ApplicantParamed Technology, Inc.
Decision Date1989-06-12
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350) is the device name listed in this FDA 510(k) record. The listed applicant is Paramed Technology, Inc.. It received FDA 510(k) clearance on 1989-06-12 under 510(k) number K890198. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350)?

PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350) is a medical device that received FDA 510(k) clearance on 1989-06-12. The listed applicant is Paramed Technology, Inc.. The 510(k) number is K890198.

When did PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350) receive FDA 510(k) clearance?

PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350) received FDA 510(k) clearance on 1989-06-12, under 510(k) number K890198.

Who is the listed applicant for PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350)?

The FDA 510(k) record lists Paramed Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350)?

The FDA product code for PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350) is DXN.

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Other records listing Paramed Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K830682CARDIVAN BLOOD PRESSURE MONITORK792226CARDIVAN BLOOD PRESSURE MONITOR

Related Devices (Code: DXN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261929Upper Arm Blood pressure monitor (BP7155D)OMRON Healthcare, Inc.K254000Happy Health Blood Pressure MonitorHappy Health, Inc.K262658Automatic Digital Blood Pressure monitor (LD-526)Honsun (Nantong) Co., Ltd.K261394Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus, DBP-61E3 Plus, DBP-61E2 Plus, DBP-62E3B Plus, DBP-62E2B Plus)JOYTECH Healthcare Co., Ltd.K253425Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6194-P,DBP-6294B-P,DBP-6195P,DBP-6295B-P, DBP-6196P,DBP-6296B-P,DBP-61E1-P, DBP-62E1B-P,DBP-62E3B-P,DBP-61E2-P,DBP-62E2B-P,DBP-61E3-P,DBP-6173-P,DBP-6273B-P,DBP-6179-P,DBP-6279B-P)Joytech Healthcare Co. , Ltd.K261061BP Go (BPP-855)Wellvii, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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